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The results of the biodistribution studies exhibit a maximum accumulation of the drug in the liver, kidney and spleen after intravenous administration of a plain drug.
Gate-dependent dI/dV spectra of graphene on hBN from STM studies exhibit a significant reduction in local microscopic charge inhomogeneity (Figure 2C).
The values of k obtained in these studies exhibit a large, up to an order of magnitude, variability that is commonly attributed to the variations in the computational setups adopted in different studies.
However, these studies exhibit a distinct phylogenetic bias: the vast majority of arthropod genomic data available have been generated for the holometabolous insects, which undergo complete metamorphosis.
Studies in experimental models provide a foundation for the clinical studies but results should be interpreted cautiously since the experimental models of diabetes, duration and type of antioxidant treatment and markers of oxidative stress investigated in these studies exhibit a wide range.
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Inequality in status-oriented higher education (mainly college and graduate studies) exhibits a wider gap than survival-based higher education (mainly adult education and junior college education).
Potency studies exhibited a PD50 of about 107 pfu/animal while a dose of 4×107pfu/animal fully protected swine against FMDV intradermal challenge.
In vitro dissolution studies exhibited a significant enhancement in dissolution rate of the drug from nanogel (85.73%) in comparison to the NTZ marketed gel (70.55%) after 24 h.
All studies exhibited a strong standard of reporting and used appropriate statistical tests.
All volunteers in those studies exhibited a significant reduction of blood pressure and heart rate.
In vitro studies exhibited a significant decrease in bone resorption by osteoclasts from CD44−/− mice.
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